Variant report

Variant	nsv883100
Chromosome Location	chr5:166718807-166808602
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:388)
CpG islands
(count:489)
Chromatin interactive
region (count:3)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:388 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr5:166785635-166786730	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr5:166785659-166786542	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr5:166721822-166722781	A549	lung:	n/a	n/a
4	BACH1	chr5:166782339-166782759	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr5:166721848-166722270	H1-hESC	embryonic stem cell:	n/a	n/a
6	BRCA1	chr5:166721778-166722989	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr5:166732947-166733196	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr5:166739284-166739598	Hela-S3	cervix:	n/a	chr5:166739436-166739447
9	CEBPB	chr5:166721784-166723084	A549	lung:	n/a	chr5:166721951-166721963 chr5:166722349-166722360
10	CEBPB	chr5:166745716-166745903	A549	lung:	n/a	n/a
11	CEBPB	chr5:166723687-166724057	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr5:166762575-166762616	HepG2	liver:	n/a	chr5:166762578-166762589 chr5:166762580-166762591
13	CEBPB	chr5:166721947-166722941	A549	lung:	n/a	chr5:166721951-166721963 chr5:166722349-166722360
14	CEBPB	chr5:166721928-166722471	H1-hESC	embryonic stem cell:	n/a	chr5:166721951-166721963 chr5:166722349-166722360
15	CEBPB	chr5:166739278-166739610	HepG2	liver:	n/a	chr5:166739436-166739447
16	CEBPB	chr5:166740201-166740363	HepG2	liver:	n/a	chr5:166740263-166740274
17	CEBPB	chr5:166739316-166739586	A549	lung:	n/a	chr5:166739436-166739447
18	CEBPB	chr5:166785970-166786430	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr5:166754731-166754836	A549	lung:	n/a	n/a
20	CEBPB	chr5:166722186-166722532	HepG2	liver:	n/a	chr5:166722349-166722360
21	CEBPB	chr5:166721721-166723014	Hela-S3	cervix:	n/a	chr5:166721951-166721963 chr5:166722349-166722360
22	CEBPB	chr5:166721769-166722953	IMR90	lung:	n/a	chr5:166721951-166721963 chr5:166722349-166722360
23	CEBPB	chr5:166762517-166762703	A549	lung:	n/a	chr5:166762578-166762589 chr5:166762580-166762591
24	CHD2	chr5:166785750-166786417	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr5:166721570-166722857	Hela-S3	cervix:	n/a	n/a
26	CHD2	chr5:166723718-166724050	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr5:166744800-166744950	AG10803	skin:	n/a	n/a
28	CTCF	chr5:166722500-166722650	A549	lung:	n/a	n/a
29	CTCF	chr5:166744860-166745010	HPAF	blood vessel:	n/a	n/a
30	CTCF	chr5:166744880-166745030	HPF	lung:	n/a	n/a
31	CTCF	chr5:166744759-166745080	IMR90	lung:	n/a	n/a
32	CTCF	chr5:166744495-166745297	A549	lung:	n/a	n/a
33	CTCF	chr5:166744920-166745070	AG09309	skin:	n/a	n/a
34	CTCF	chr5:166732240-166732390	HEEpiC	esophagus:	n/a	n/a
35	CTCF	chr5:166744740-166744890	NHLF	lung:	n/a	n/a
36	CTCF	chr5:166744796-166745051	A549	lung:	n/a	n/a
37	CTCF	chr5:166744893-166744962	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr5:166744840-166744990	AG04449	skin:	n/a	n/a
39	CTCF	chr5:166744840-166744990	HEK293	kidney:	n/a	n/a
40	CTCF	chr5:166750129-166750245	K562	blood:	n/a	n/a
41	CTCF	chr5:166744880-166745030	MCF-7	breast:	n/a	n/a
42	CTCF	chr5:166744918-166744979	GM12878	blood:	n/a	n/a
43	CTCF	chr5:166744876-166744951	MCF-7	breast:	n/a	n/a
44	CTCF	chr5:166800860-166801010	HA-sp	spinal cord:	n/a	n/a
45	CTCF	chr5:166744860-166745010	BJ	skin:	n/a	n/a
46	CTCF	chr5:166744820-166744970	AG10803	skin:	n/a	n/a
47	CTCF	chr5:166744900-166745050	A549	lung:	n/a	n/a
48	CTCF	chr5:166744840-166744990	AG09319	gingival:	n/a	n/a
49	CTCF	chr5:166725460-166725516	GM20000	blood:	n/a	n/a
50	CTCF	chr5:166744900-166745050	WI-38	lung:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:166745042-166745092	GM12891	blood:	n/a
2	chr5:166745042-166745092	GM12891	blood:	n/a
3	chr5:166802258-166802308	MCF-7	breast:	n/a
4	chr5:166782271-166782321	PANC-1	pancreas:	n/a
5	chr5:166802425-166802475	AG04449	skin:	fetal
6	chr5:166782271-166782321	HL-60	blood:	n/a
7	chr5:166802425-166802475	HCT-116	colon:	n/a
8	chr5:166802870-166802920	SAEC	small airway:	n/a
9	chr5:166782271-166782321	Jurkat	blood:	n/a
10	chr5:166722513-166722563	SKMC	muscle:	n/a
11	chr5:166732608-166732658	GM12891	blood:	n/a
12	chr5:166802870-166802920	Hepatocyte	liver:	n/a
13	chr5:166802425-166802475	Hepatocyte	liver:	n/a
14	chr5:166722513-166722563	U87	brain:	n/a
15	chr5:166732608-166732658	H1-hESC	embryonic stem cell:	embryo
16	chr5:166802318-166802368	CMK	blood:	n/a
17	chr5:166732608-166732658	ECC-1	luminal epithelium:	n/a
18	chr5:166745042-166745092	ProgFib	skin:	n/a
19	chr5:166782271-166782321	LNCaP	prostate:	n/a
20	chr5:166802870-166802920	HEK293	kidney:	embryo
21	chr5:166802258-166802308	BJ	skin:	n/a
22	chr5:166782271-166782321	NH-A	brain:	n/a
23	chr5:166745042-166745092	NHBE	bronchial:	n/a
24	chr5:166782271-166782321	GM06990	blood:	n/a
25	chr5:166745042-166745092	GM19239	blood:	n/a
26	chr5:166782271-166782321	SK-N-SH	brain:	n/a
27	chr5:166782271-166782321	T-47D	breast:	n/a
28	chr5:166722513-166722563	AG04449	skin:	fetal
29	chr5:166802258-166802308	Hepatocyte	liver:	n/a
30	chr5:166722513-166722563	AoSMC	blood vessel:	n/a
31	chr5:166802870-166802920	MCF-7	breast:	n/a
32	chr5:166802870-166802920	GM12892	blood:	n/a
33	chr5:166802870-166802920	BJ	skin:	n/a
34	chr5:166802425-166802475	GM06990	blood:	n/a
35	chr5:166722513-166722563	HMEC	breast:	n/a
36	chr5:166782271-166782321	SAEC	small airway:	n/a
37	chr5:166722513-166722563	SAEC	small airway:	n/a
38	chr5:166802258-166802308	SK-N-MC	brain:	n/a
39	chr5:166802425-166802475	PFSK-1	brain:	n/a
40	chr5:166722513-166722563	NB4	blood:	n/a
41	chr5:166802870-166802920	HCT-116	colon:	n/a
42	chr5:166802318-166802368	MCF-7	breast:	n/a
43	chr5:166802425-166802475	CMK	blood:	n/a
44	chr5:166802318-166802368	HIPEpiC	eye:	n/a
45	chr5:166745042-166745092	HEK293	kidney:	embryo
46	chr5:166732608-166732658	Caco-2	colon:	n/a
47	chr5:166802425-166802475	HRPEpiC	eye:	n/a
48	chr5:166802870-166802920	HMEC	breast:	n/a
49	chr5:166782271-166782321	IMR90	lung:	fetal
50	chr5:166802425-166802475	MCF10A-Er-Src	breast:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:61184757..61185584-chr5:166788286..166789011,2	MCF-7	breast:
2	chr5:166761474..166763791-chr5:166767248..166768863,2	K562	blood:
3	chr5:166761474..166763791-chr5:166767248..166768863,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PANK3-7	chr5:166733278-166733616	ENSG00000253527.1
2	lnc-PANK3-9	chr5:166721256-166721278	ENSG00000254365.1
3	lnc-PANK3-7	chr5:166736804-166736875	ENSG00000253527.1
4	lnc-PANK3-8	chr5:166724468-166724555	ENSG00000254297.1
5	lnc-PANK3-8	chr5:166723239-166723548	ENSG00000254297.1
6	lnc-PANK3-7	chr5:166734941-166735056	ENSG00000253527.1
7	lnc-PANK3-8	chr5:166730128-166730377	ENSG00000254297.1

No data

Variant related genes	Relation type
ENSG00000253527	TF binding region
ENSG00000254365	TF binding region
ENSG00000254297	TF binding region
ENSG00000253527	CpG island
ENSG00000254365	CpG island
ENSG00000254297	CpG island

Extended variants
information (count: 2919 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:2919 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7731005	chr5:166718807-166718808	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs554604837	chr5:166718855-166718856	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs542223221	chr5:166718856-166718857	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs112021736	chr5:166719025-166719026	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs562438423	chr5:166719074-166719075	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs145615542	chr5:166719163-166719164	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs113636873	chr5:166719167-166719168	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs72645736	chr5:166719256-166719257	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs533307404	chr5:166719318-166719319	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs192217273	chr5:166719335-166719336	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs142592424	chr5:166719350-166719351	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs150989769	chr5:166719365-166719366	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs549089782	chr5:166719474-166719475	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567599430	chr5:166719541-166719542	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs537742640	chr5:166719596-166719597	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs532258781	chr5:166719599-166719600	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs577916907	chr5:166719629-166719630	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs142030018	chr5:166719664-166719665	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs372391596	chr5:166719758-166719759	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs553919820	chr5:166719788-166719789	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs572030318	chr5:166719790-166719791	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs376731134	chr5:166719873-166719874	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs184063536	chr5:166719920-166719921	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs145857773	chr5:166719953-166719954	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs185853320	chr5:166719957-166719958	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs547419186	chr5:166719988-166719989	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs562792403	chr5:166719996-166719997	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs545576725	chr5:166720000-166720001	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs533367603	chr5:166720024-166720025	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs545183418	chr5:166720028-166720029	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs112938030	chr5:166720065-166720066	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs563875950	chr5:166720100-166720101	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs531176163	chr5:166720170-166720171	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs201907935	chr5:166720181-166720182	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs190502170	chr5:166720209-166720210	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs113713760	chr5:166720223-166720224	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs527782685	chr5:166720226-166720227	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs549636400	chr5:166720232-166720233	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs182385763	chr5:166720247-166720248	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs567893050	chr5:166720261-166720262	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs386694645	chr5:166720263-166720264	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs386694646	chr5:166720265-166720266	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs563323016	chr5:166720267-166720268	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs538869992	chr5:166720292-166720293	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs187066590	chr5:166720310-166720311	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs377559498	chr5:166720315-166720316	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs34907290	chr5:166720327-166720328	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs565813037	chr5:166720371-166720372	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs373790909	chr5:166720374-166720375	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs570735848	chr5:166720417-166720418	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Breast cancer	17603634	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
severe myoclonic epilepsy of infancy	18294202	CNVD
Olfactory neuroblastoma	18408657	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mental retardation	17124404	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:544 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:166709400-166719800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr5:166714200-166719800	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr5:166714800-166721600	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr5:166715000-166719200	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr5:166715000-166720800	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr5:166715000-166722200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr5:166715000-166722400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr5:166718000-166719000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr5:166718400-166720200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
10	chr5:166718600-166720200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
11	chr5:166718800-166722400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr5:166718800-166722400	Weak transcription	Aorta	Aorta
13	chr5:166719000-166721000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr5:166719200-166719800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
15	chr5:166719800-166720000	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
16	chr5:166719800-166720000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr5:166719800-166720800	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr5:166719800-166721200	Strong transcription	H9 Cell Line	embryonic stem cell
19	chr5:166719800-166722000	Enhancers	Hela-S3	cervix
20	chr5:166720000-166722200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
21	chr5:166720000-166722200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr5:166720200-166720800	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr5:166720200-166721000	Strong transcription	ES-I3 Cell Line	embryonic stem cell
24	chr5:166720400-166724000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr5:166720600-166724000	Enhancers	Fetal Lung	lung
26	chr5:166720800-166721400	Genic enhancers	HUES6 Cell Line	embryonic stem cell
27	chr5:166720800-166721600	Enhancers	A549	lung
28	chr5:166720800-166722200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr5:166720800-166722400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr5:166720800-166722400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr5:166720800-166724600	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr5:166720800-166724600	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr5:166720800-166724800	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr5:166721000-166722200	Genic enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr5:166721000-166722200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr5:166721000-166722200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr5:166721000-166722200	Enhancers	HMEC	breast
38	chr5:166721000-166722200	Enhancers	HUVEC	blood vessel
39	chr5:166721000-166722600	Enhancers	Rectal Mucosa Donor 29	rectum
40	chr5:166721000-166723000	Enhancers	Ovary	ovary
41	chr5:166721000-166724400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr5:166721000-166724600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr5:166721000-166724600	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr5:166721200-166721800	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr5:166721200-166722000	Enhancers	Small Intestine	intestine
46	chr5:166721200-166722000	Enhancers	NHEK	skin
47	chr5:166721200-166722200	Enhancers	NHLF	lung
48	chr5:166721200-166723000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr5:166721200-166723800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr5:166721400-166721600	Enhancers	NH-A	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links